A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053470



Internal ID18796001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46975048..47103613hg19UCSC Ensembl
Innerchr10:46395054..46523619hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19128566
hg18128566
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv763n100
Supporting Variantsnssv3522488
Samples
Known GenesGPRIN2, LINC00842, LOC100996758, NPY4R
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053470
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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